Splinted ligation adapter tagging

ABSTRACT

A method is provided comprising the following steps: (a) treating a nucleic acid with bisulfite to convert non-methylated cytosines in the nucleic acid into uracils while leaving methylated cytosines unchanged to form a treated nucleic acid strand that is part of two joined nucleic acid strands; (b) ligating a first adapter to a 3′ end of the treated nucleic acid strand, the first adapter having a first protruding random sequence that least 3 bases long and that acts as a splint for the two joined nucleic acid strands; (c) ligating a second adapter to a 5′ end of the once adapter ligated nucleic acid strand, the second adapter having a second protruding random sequence at least 3 bases long and that acts as a splint for the two joined nucleic acid strands; and (d) performing PCR amplification on the twice ligated nucleic acid strand.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application makes reference to and claims the priority benefit ofthe following U.S. Provisional Patent Application No. 62/580,465 filedNov. 2, 2017. The entire disclosure and contents of the foregoingProvisional application is hereby incorporated by reference.

FIELD OF THE INVENTION

The invention relates to methods for quantitative detection of DNAsequences, their incorporation in DNA libraries, and uses thereof

BACKGROUND

For decades, researchers have used Southern and Northern blotting todetect DNA and RNA sequences, respectively, in samples. These and othertools for analysis have developed over time to offer faster, easier, andmore reliable approaches. Next Generation Sequencing (NGS), also knownas Massive Parallel Sequencing (MPS), has recently emerged as a powerfultool for analysis of nucleic acids.

Splinted ligation technology is introduced in 2003 as a protocol fordirect labeling and subsequent quantitative detection of small RNAsequences (see Moore M. J. and Query C. C., “Joining of RNAs by SplintedLigation,” Methods Enzymol 2000, 317:2003). In splinted ligation, two ormore RNA fragments are joined using bridging splint DNA templates, thuscreating complexes nicked at the ligation substrate site. Despite theabsence of an amplification step, the protocol yields results at leastfifty times more sensitive than those from Northern blots, making RNAdetection from extremely small samples now possible.

Sequence tagging technology is predominantly used for RNA analysis.However, it has been modified for use with DNA (see Gansauge M. T. andMeyer M., Nature Protocols 8, 737-748 (2013) and Gansauge et al.“Single-Stranded DNA Library Preparation from Highly Degraded DNA SsingT4 DNA Ligase,” Nucleic Acids Res 2017). But despite these advances insequence tagging technology, there remains a need in the art forprotocols which offer sensitive and straightforward methods forpreparing DNA libraries.

SUMMARY

According to a first broad aspect of the present invention, there isprovided a method comprising the following steps: (a) treating a nucleicacid with bisulfite to convert non-methylated cytosines in the nucleicacid into uracils while leaving methylated cytosines unchanged to form atreated nucleic acid strand that is part of two joined nucleic acidstrands; (b) ligating a first adapter to a 3′ end of the treated nucleicacid strand to thereby form a once adapter ligated nucleic acid strand,the first adapter having a first protruding random sequence that is atleast 3 bases long and that acts as a splint for the two joined nucleicacid strands; (c) ligating a second adapter to a 5′ end of the onceadapter ligated nucleic acid strand to thereby form a twice ligatednucleic acid strand, the second adapter having a second protrudingrandom sequence that is at least 3 bases long and that acts as a splintfor the two joined nucleic acid strands; and (d) performing polymerasechain reaction (PCR) amplification on the twice ligated nucleic acidstrand to thereby generate copies of the twice ligated nucleic acidstrand.

BRIEF DESCRIPTION OF THE DRAWINGS

The invention will be described in conjunction with the accompanyingdrawings, in which:

FIG. 1 is a diagram showing three prior library preparation methods(Prior Methods 1 through 3) for whole genome bisulphite sequencing, aswell as a method for library preparation according to one embodiment ofthe present invention;

FIG. 2 is a flowchart showing whole genome bisulphite sequencing (WGBS)process according to one embodiment of the present invention;

FIG. 3 are graphical base sequence content plots for a prior WGBSmethod, as well as for one embodiment of the method of the presentinvention generated by the FastQC program wherein the Y axis representsthe % of all bases and the X axis represents the position in the read;

FIG. 4 are graphical base sequence content plots for two prior WGBSmethods generated by the FastQC program;

FIG. 5 are graphical size profile plots of WGBS libraries generated byone prior WGBS method, as well as by one embodiment of the method of thepresent invention, wherein the Y-axis represents sample intensity (inFluorescence Units) and the X-axis represents the size (in terms of basepairs);

FIG. 6 are graphical size profile plots of WGBS libraries generated bytwo prior WGBS methods;

FIG. 7 are graphical size profile plots of eight SPLAT librariesgenerated from the lymphoblastoid cell lines NA11992 and NA11993;

FIG. 8 is a table showing sequence metrics for whole genome bisulfitelibraries;

FIG. 9 is a table showing read coverage and correlation of methylationbetween SPLAT and high coverage reference data;

FIG. 10 are graphical plots of read coverage histograms for an NA10860sample, wherein the Y-axis represents the fraction of the genome, andthe X-axis represents coverage (i.e., read counts);

FIG. 11 is a table showing correlation of DNA methylation levels of CpGsites with binned coverage in SPLAT with the high coverage referencelibraries;

FIG. 12 are two graphical plots providing a comparison of methylationlevels at individual CpG sites located throughout known imprintedregions in the high coverage reference data sets (y axis) and in SPLATlibraries (x-axis);

FIG. 13 are graphical plot comparisons of SPLAT with a high coveragereference dataset including: scatter plots showing a pairwise comparisonof methylation levels at individual CpG sites in CpG islands, enhancers,and repetitive regions determined by SPLAT (x-axis) and thehigh-coverage reference WGBS data (y-axis) obtained by combining thedata from TruSeq DNA Methylation, Accel-NGS and NEBNextUltra librarieswith Pearson's correlation coefficients shown in the lower right cornerof each scatter plot, two tables showing the mean read coverage of theCpG sites in CpG islands, enhancers and repeats for SPLAT and the highcoverage reference data set, diagrams comparing the numbers and overlapsof un-methylated regions (UMRs) between SPLAT and high coveragereference WGBS data, and diagrams comparing the numbers and overlaps oflowly methylated regions (LMRs) in SPLAT and high coverage referenceWGBS data, wherein in the Scatter plots (1312-1316), the darker areasrepresent where there are many CpG sites with similar or the samemethylation values detected in the reference (Y axis) and SPLAT(X-axis), and which shows that there is a strong correlation, i.e., thatSPLAT produces the same DNA methylation measurements as the referencedataset, and wherein in the Venn diagrams (1350-1380), each circlerepresents a number of a specific type or region found in the respectivedata sets, “LMRs” (or “UMRs”) being colored by data set, wherein thepart of the circles that overlap illustrates the degree of overlapbetween the two data sets, i.e., how many were found in both datasets,and wherein the non-overlapping portions of the circles represent thefraction of LMRs found only in the one data set;

FIG. 14 is a table showing performance metrics for various WGBS librarypreparation methods, including a WGBS library preparation methodaccording to one embodiment of the present invention;

FIG. 15 are GC profile and coverage plots for various sequencing librarypreparation methods, including a method according to one embodiment ofthe present invention, wherein the Y-axis represents the fraction of thefeature (i.e., features=genome, enhancers, CpG islands or difficultpromoters, each represented by a differently colored line), and whereinthe X-axis represents coverage (i.e., read count);

FIG. 16 are graphs of: read coverage and methylation levels across a 3.5Mb region of chromosome 12, a zoom-in view of a CpG poor 7.3 kbintergenic region on chromosome 12 and zoom-in view of a 6.4 kb regioncontaining a methylated CpG island on chromosome 19 for varioussequencing library preparation methods, including a method according toone embodiment of the present invention;

FIG. 17 are graphical coverage profile plots of public WGBS data setsdownloaded from the short read archive (SRA), including TruSeq DNAMethylation libraries from lymphoblastoid cell line NA18507 (Accession#SRR1867799, SRR1867802, SRR1818296) and conventional WGBS librariesamplified with the KAPA HiFi Uracil polymerase, wherein the Y-axisrepresents the fraction of the feature (i.e., features=genome,enhancers, CpG islands or difficult promoters, each represented by adifferently colored line), and wherein the X-axis represents coverage(i.e., read count);

FIG. 18 is a table showing global methylation levels in the CHG and CHH(where H represents either A, T or C but not G) sequence context are low(0.3-1%), indicating that the bisulphite conversion rates are >99% inall libraries;

FIG. 19 is a table showing average methylation across mitochondrial CpGsites;

FIG. 20 is a table showing a summary of within read methylation for ananalysis of individual reads with two or more CpG sites;

FIG. 21 are graphical plots showing Mbias profiles for visualization ofmethylation biases across NGS reads;

FIG. 22 is a table showing correlation coefficients for comparisonbetween technical replicates for various WGBS method;

FIG. 23 is a table showing reduced-representation-bisulphite-sequencing(RRBS) and SureSelect MethylSeq libraries;

FIG. 24 is a set of graphical scatterplots showing the correlation ofaverage methylation in CpG Islands, across WGBS library preparationmethods;

FIG. 25 is a set of graphical scatterplots showing average methylationin enhancer regions in scatterplots showing the correlation of averagemethylation in FANTOM5 enhancer regions, across WGBS library preparationmethods, wherein the Y axis represents % methylation in the dataset andthe X-axis represents % methylation in the dataset;

FIG. 26 are correlation matrixes showing pairwise comparison ofmethylation levels at individual CpG sites with, Pearson's correlationcoefficients shown to the left of the diagonal, as well as Venn diagramsshowing overlap of unmethylated and lowly methylated regions in threepost bisulfite methods;

FIG. 27 is a table which shows numbers of low- and un-methylated regionsas identified by MethylSeekR;

FIG. 28 is a table showing the read coverage of CpG sites in differentWGBS libraries;

FIG. 29 is a table showing the annotation of low coverage CpGs (coveredby two or fewer reads) to genomic features in NEBNextUltra libraries(216-219 M read pairs analyzed);

FIG. 30 are bar graphs showing a annotation of CpG sites with lowcoverage in the ‘post bisulphite’ WGBS methods; and

FIG. 31 is a table showing a comparison of the characteristics ofdifferent WGBS library preparation technologies.

DETAILED DESCRIPTION

It is advantageous to define several terms before describing theinvention. It should be appreciated that the following definitions areused throughout this application.

Definitions

Where the definition of terms departs from the commonly used meaning ofthe term, applicant intends to utilize the definitions provided below,unless specifically indicated.

For the purposes of the present invention, directional terms such as“top,” “bottom,” “side,” “front,” “frontal,” “forward,” “rear,”“rearward,” “back,” “trailing,” “above”, “below”, “left”, “right”,“horizontal”, “vertical”, “upward”, “downward”, etc. are merely used forconvenience in describing the various embodiments of the presentinvention.

For purposes of the present invention, the term “adapter” refers to ashort single stranded or double stranded oligonucleotide of at least 3bases, for example, 3 to 70 bases, such as 13 to 25 bases, that can beligated to the ends of other DNA or RNA molecules.

For purposes of the present invention, the term “adapter tagging” refersto the ligation of adapters to nucleic acids with the aim to producenucleic acids with 3′ and 5′tags containing known sequences, in turnenabling detection or further analysis by next generation sequencing orby other nucleic acid detection technologies.

For purposes of the present invention, the term “bisulphite”(interchangeable with the term “bisulfite”) refers to the conventionalmeaning of the term “bisulphite”, i.e., any salt including the ion HSO₃⁻ ion. An example of a bisulphite salt is sodium bisulphite.

For purposes of the present invention, the term “bisulphite-convertedDNA” refers to DNA which has been treated with a bisulphite to convert aDNA's non-methylated cytosines into uracils, leaving methylatedcytosines unchanged.

For purposes of the present invention, the term “DNA” refers todouble-stranded (ds) and single-stranded (ss) DNA, unless specifiedotherwise and may refer to an entire DNA molecule or strand of DNA or asegment of a DNA molecule or strand of DNA, unless specified otherwise.

For purposes of the present invention, the term “nucleic acid” refers toany molecule that comprises nucleotides linked in a chain. Examples ofnucleic acids are DNA and RNA.

For purposes of the present invention, the term “oligonucleotide” refersto the conventional meaning of the term “oligonucleotide”, i.e., a shortchain nucleic acid polymer of at least 3, for example from 3 to 70, suchas from 13 to 25, nucleic acids in length.

For purposes of the present invention, the term “polymerase chainreaction (PCR) amplification” refers to the conventional meaning to theterm PCR amplification, i.e., a technique used in molecular biology toamplify a single copy or a few copies of a segment of DNA across severalorders of magnitude, generating thousands to millions of copies of aparticular DNA sequence.

For purposes of the present invention, the term “protruding randomsequence” refers to a portion of an adapter that is a random sequence ofbases and that extends beyond one of a pair of joined nucleic acidstrands for which the adapter acts as a splint. In one embodiment of thepresent invention, the protruding random sequence of an adapter being atleast 3 bases long, such as from 3 to 20 bases long.

For purposes of the present invention, the term “shearing” refers toforming a fragment of a nucleic acid from a nucleic acid or a fragmentof a nucleic acid that is smaller than the original nucleic acid orfragment of a nucleic acid that is sheared. Shearing techniques that maybe used in the various embodiments of the method of the presentinvention include: acoustic shearing, sonication, hydrodynamic shearing,enzymatic shearing, chemical shearing, heat induced shearing, etc.

For purposes of the present invention, the term “ligation” refers to theconventional meaning of this term as the covalent linking of two ends ofDNA or RNA molecules, most commonly done using DNA ligase, RNA ligase(ATP) or other enzymes.

For purposes of the present invention, the term “splinted ligation”refers to the conventional meaning of this term as the joining of two ormore RNA (or DNA) fragments by including bridging splint DNA templatesto create RNA:RNA/DNA (or DNA:DNA/DNA) complexes which are nickedspecifically at the desired site of the ligation substrate.

For purposes of the present invention, the term “bridging splint DNAtemplates” refers to nucleic acids used for bringing two nucleic acidstogether by use of a splinted bridging sequence.

For purposes of the present invention, the term “DNA library” refers tothe conventional meaning of this term as a collection of DNA fragmentsthat may be sequenced on a next generation sequencer. The fragments thatmay be sequenced on a next generation sequencer may also be stored andpropagated in a population of microorganisms through the process ofmolecular cloning.

For purposes of the present invention, the term “non-methylatedcytosine” refers to cytosine which are converted to uracil through aprocess of deamination (i.e., the removal of an amino group).

For purposes of the present invention, the term “methylated cytosine”refers to cytosine which has been methylated (e.g., 5-methylcytosine)and which therefore cannot be converted to uracil through a process ofdeamination.

For purposes of the present invention, the terms “bisulphite sequencing”or “bisulfite sequencing” refer to the use of bisulphite/bisulfitetreatment of DNA or RNA to determine its pattern of methylation.

For purposes of the present invention, the term “whole genome bisulphitesequencing” (hereafter referred to interchangeably as “WGBS”) refers tosequencing of bisulfite converted DNA with next generation sequencing(NGS) to determine patterns of DNA methylation in the genome.

For purposes of the present invention, the term “SPlinted LigationAdapter Tagging” (hereafter referred to interchangeably as “SPLAT”)refers to the process of creating sequencing libraries fromsingle-stranded nucleic acids by use of splinted ligation.

For purposes of the present invention, the term “oligo annealing” refersto the coming together of a short sequence of complementary nucleicacids to a nucleic acid template.

For purposes of the present invention, the term “next generationsequencing” (hereafter referred to interchangeably as “NGS,” and alsoknown as interchangeably as Massive Parallel Sequencing (MPS)) nominallyrefers to non-Sanger-based high-throughput DNA sequencing technologieswhere millions or even billions of DNA molecules may be sequenced inparallel, yielding substantially more throughput and minimizing the needfor the fragment-cloning methods that are often used in Sanger-basedsequencing of genomes.

For purposes of the present invention, the term “TruSeq DNA Methylation”refers to a commercially available WGBS library preparation protocolfrom Illumina, Inc.

For purposes of the present invention, the term “Accel-NGS Methyl-Seq”refers to a commercially available WGBS library preparation protocolfrom Swift Biosciences.

For purposes of the present invention, the term “RRBS” refers to reducedrepresentation bisulfite/bisulphite sequencing.

For purposes of the present invention, the term “SureSelect Methyl-Seq”refers to commercially available targeted bisulfate/bisulphitesequencing protocol from Agilent Technologies.

For purposes of the present invention, the term “CpG” refers to a regionof DNA where a cytosine nucleotide is adjacent to a guanine nucleotidein the 5′->3′ direction. Accordingly, the term “CpG sites” refers tomultiple CpGs, while the term “CpG islands” refers to regions of thegenome where there is an overrepresentation of CpGs, typically theregion is >200 bp long with >50% cytosine and guanine nucleotides.

For purposes of the present invention, the term “targeted capturemethods” refers to methods where specific regions of the genome areenriched in a sequencing library.

For purposes of the present invention, the term “solution hybridizationprotocols” refers to targeted capture methods that are performed insolution.

For purposes of the present invention, the term “tagmentation-basedwhole genome bisulphite sequencing” (hereafter interchangeably referredto as “T-WGBS”) refers to a WGBS library preparation method whereadapters are ligated to double stranded DNA with the help of the Tn5enzyme.

For the purposes of the present invention, the term “liquid” refers to anon-gaseous fluid composition, compound, material, etc., which may bereadily flowable at the temperature of use (e.g., room temperature) withlittle or no tendency to disperse and with a relatively highcompressibility.

For the purposes of the present invention, the term “room temperature”refers to the commonly accepted meaning of room temperature, i.e., anambient temperature of 20° to 25° C.

For the purposes of the present invention, the term “comprising” meansvarious compositions, compounds, components, elements, steps, etc., maybe conjointly employed in embodiments of the present invention.Accordingly, the term “comprising” encompasses the more restrictiveterms “consisting essentially of” and “consisting of.”

For the purposes of the present invention, the terms “a” and “an” andsimilar phrases are to be interpreted as “at least one” and “one ormore.” References to “an” embodiment in this disclosure are notnecessarily to the same embodiment.

For the purposes of the present invention, the term “and/or” means thatone or more of the various compositions, compounds, components,elements, steps, etc., may be employed in embodiments of the presentinvention.

Unless otherwise specified, all percentages given herein are by weight.

Description

Sodium bisulphite treatment converts DNA's non-methylated cytosines intouracils, leaving methylated cytosines unchanged. Hence, methylationstatus at individual CpG sites can be read out by next generationsequencing. However, the strand-breaking side effect of sodium bisulfitetreatment makes traditional methods of library preparation inefficient.Moreover, after bisulfite treatment the DNA is single stranded (ssDNA).High DNA input amounts are required to produce bisulfite sequencinglibraries according to standard protocols, which may be prohibitive,e.g., methylation analysis using clinical samples.

The initial bisulphite treatment of the DNA, followed by adapter taggingof single stranded DNA (ss DNA) fragments, enables whole genomebisulphite sequencing (WGBS) using low quantities of input DNA.

It has surprisingly been found that a library preparation methodaccording to one embodiment of the present invention can be based on theuse of adapters with degenerate splints for ligation to single-strandedbisulfite-converted DNA. After oligo annealing, short stretches of dsDNAare produced and the ssDNA molecule is efficiently ligated to thesequencing adapter using standard T4 DNA ligase. This enables librarypreparation even with small amounts of DNA. Although in the describedembodiment of the present invention, the protocol has been optimized forbisulfite converted DNA, in theory any single stranded DNA (ssDNA) maycaptured in to a sequencing library with this method. (The variousprocesses and procedures that may be used in embodiments of the methodof the present invention are also described and shown in Raine et al.,“SPlinted Ligation Adapter Tagging (SPLAT), a Novel Library PreparationMethod for Whole Genome Bisulphite Sequencing,” Nucleic Acids Research,2017, Vol. 45, No. 6, e36, the entire contents and disclosure of whichis incorporated herein by reference.) While embodiments of the method ofthe present invention are applicable to all manner of ssDNA analysis,described in detail herein is a method according to one embodiment ofthe present invention of particular utility for analysis ofbisulphite-converted DNA.)

Additionally, sodium bisulphite treatment of DNA combined with nextgeneration sequencing (NGS) is a powerful combination for theinterrogation of genome-wide DNA methylation profiles. Librarypreparation for WGBS is challenging due to side effects of thebisulphite treatment, which may lead to extensive DNA damage in the formof strand breakage. Recently, a new generation of methods for bisulphitesequencing library preparation have been devised. These methods forbisulphite sequencing library preparation are based on initialbisulphite treatment of the DNA, followed by adapter tagging of singlestranded DNA (ssDNA) fragments, and enable WGBS using low quantities ofinput DNA. In one embodiment, the present invention presents a novelapproach for quick and cost-effective WGBS library preparation that isbased on splinted adapter tagging (SPLAT) of bisulphite-convertedsingle-stranded DNA. In the examples described below, embodiments of themethod of the present invention are compared against three commerciallyavailable WGBS library preparation techniques, two of which are based onbisulphite treatment prior to adapter tagging and one of which is aconventional WGBS method. Indeed, as further evidence of the unique andnon-obvious nature of some embodiments of the method the presentinvention, an example is described below which provides a validation ofan embodiment of the method of the present invention against threecommercially-available WGBS library preparation techniques, two of whichrely on bisulphite treatment (TruSeq DNA Methylation, Accel-NGSMethyl-Seq, and RRBS, target capture by SureSelect Methyl-Seq, and 450 kBeadArrays).

Also, methylation of cytosine (5-mC) residues in CpG dinucleotides is anepigenetic modification that plays a pivotal role in the establishmentof cellular identity by influencing gene expression. In somaticmammalian cells, the majority of CpG sites are methylated. However, CpGsites located in regions of increased CG density, known as CpG islands,generally have low levels of CpG methylation (1). On the molecularlevel, it is well known that CpG methylation leads to X-chromosomeinactivation, genomic imprinting, regulation of gene expression andsuppression of transposable elements. Disruption of DNA methylationpatterns is associated with disease, and particularly with cancer (2).These findings have spurred the development of technologies for genomewide DNA methylation profiling. The HumanMethylation450 BeadChip assay(450 k Bead Arrays, Illumina) has so far been the most frequently usedplatform for human studies. However, with the advent of high throughputsequencing techniques there has been a rapid development of methods thatinterrogate a larger proportion of the CpG sites in any genome, whichcan interrogate from a few million CpG sites up to the whole methylome,which in humans consists of 28 million CpG sites. Sodium bisulphitetreatment of DNA converts non-methylated cytosines into uracils, whilstmethylated cytosines remain unchanged (3). Hence, methylation status atindividual CpG sites can be read out by sequencing or genotyping (4-6).Methods for genome-wide DNA methylation analysis that rely on bisulphiteconversion of DNA include BeadArrays (7, 8)reduced-representation-bisulphite-sequencing (RRBS) (9-12), targetedcapture methods (13-16), and WGBS. The 450 k and 850 k (EPIC) BeadArraysinterrogate 2-4% of human CpG sites that are preselected based onvarious annotated features such as genes, promoters, CpG islands andregulatory elements such as enhancers. Targeted capture methods may bedesigned to interrogate any region of the genome using, e.g., bisulphitepadlock probes (13, 14) or in solution hybridization protocols (15-17).The latter is implemented in several commercial kits, such as SureSelectMethyl-Seq (Agilent Technologies) and SeqCap Epi systems (RocheNimbleGen). RRBS uses restriction enzyme digestion to enrich for regionsof high CpG content, such as CpG islands and promoters in any genome(9-12).

WGBS is the ideal choice for many DNA methylation studies since itallows for unbiased genome-wide profiling at single-base resolution.However, a drawback of WGBS is that it is still costly to perform onlarge sample sets. Moreover, conventional sample preparation methods forWGBS typically require microgram amounts of DNA, which may beprohibitive for many human disease applications and sample types, forexample, rare cell types or small tissue biopsies where obtainingmicrogram amounts of DNA is not feasible. The strand breaking sideeffect of sodium bisulphite treatment renders the majority of sequencinglibrary constructs unamplifiable during PCR and sequencing clustergeneration. Using low amounts of input DNA is feasible, albeit at theexpense of low complexity of the sequencing libraries and highredundancy of the obtained sequence reads caused by the large number ofamplification cycles required. Tagmentation-based whole genomebisulphite sequencing (T-WGBS) (18) is developed for low DNA quantitylibrary construction, but a major drawback to this approach is that thetagmentation is performed prior to bisulphite conversion and thusextensive amplification may still be required.

In order to circumvent the damage of library constructs, methods havebeen designed in which sequencing adapters are incorporated afterbisulphite treatment (hereafter referred to as ‘post bisulphite’methods) (19, 20). Various examples of such methods as well as anembodiment of the method according to the present invention are shown inFIG. 1. A conventional method is shown in column 110. AccelNGSMethyl-Seq protocol (Swift Biosciences) is shown in column 130,Illumina's TruSeq DNA Methylation kit's method is shown in column 150.The splinted adapter tagging (SPLAT) of bisulphite-convertedsingle-stranded DNA method according to one embodiment of the presentinvention is shown in column 170. In the pioneering post bisulphitemethod PBAT (post bisulphite adapter tagging) which is not shown in FIG.1 but similar in concept to the method shown in column 150, sequencingadapters are attached by two rounds of random primer extension using thebisulphite converted ssDNA as the initial template. PBAT enabledPCR-free WGBS libraries to be constructed from DNA quantities in thenanogram range (19) and has paved the way for further developments, suchas Illumina's TruSeq DNA Methylation kit shown in column 130. Notably, amodified version of the PBAT protocol is recently used for single cellmethylation profiling (21). An alternative approach for post bisulphitelibrary preparation is implemented in the AccelNGS Methyl-Seq protocol(Swift Biosciences), shown in column 130, whereby a low complexitysequence tag is added to the 3′ end of the ssDNA in order to serve as ascaffold for the attachment of sequencing adapters.

Principles of Library Preparation Methods for Whole Genome BisulphiteSequencing:

According to the conventional method (see column 110 in FIG. 1)methylated adapters are ligated to double stranded sheared DNAfragments. The constructs are then bisulphite converted prior toamplification with a uracil reading PCR polymerase. The Accel-NGSMethyl-Seq method (see column 130 in FIG. 1) uses the proprietaryAdaptase™ technology to attach a low complexity sequence tail to the3′-termini of pre-sheared and bisulphite-converted DNA, and an adaptersequence. After an extension step a second adapter is ligated and thelibraries are PCR amplified. The TruSeq DNA Methylation method (formerlyEpiGnome) (see column 150 in FIG. 1) uses random hexamer taggedoligonucleotides to simultaneously copy the bisulphite-converted strandand add a 5′-terminal adapter sequence. In a subsequent step, a3′-terminal adapter is tagged, also by using a random sequenceoligonucleotide and the libraries are PCR amplified.

In the method according to one embodiment of the present invention (seecolumn 170 in FIG. 1), sheared double stranded DNA 172 is subject to abisulphite converson at step 174 which produce bisulphite convertedsingle DNA strands 176. At step 178, adapters with a protruding randomhexamer are annealed to the 3′-termini of single stranded DNA 176. Therandom hexamer acts as a ‘splint’, indicated by arrow 180 and theadapter sequence is ligated to the 3′-termini of single stranded DNA 176using standard T4 DNA ligation. A modification of the last 3′-residue ofthe random hexamer is required to prevent self-ligation of the adapter.At step 182, adapters with a 5′-terminal random hexamer overhang isannealed to ligate the 5′-termini of single stranded DNA 176, also usingT4 DNA ligase. Finally, at step 186, the libraries are PCR amplifiedusing a uracil reading polymerase to produce DNA copies 192.

Having described the several embodiments of the present invention indetail, it will be apparent that modifications and variations arepossible without departing from the scope of the invention defined inthe appended claims. Furthermore, it should be appreciated that allexamples in the present disclosure, while illustrating many embodimentsof the invention, are provided as non-limiting examples and are,therefore, not to be taken as limiting the various aspects soillustrated.

EXAMPLES

Illustrative examples of embodiments of the present invention aredescribed below:

Example 1

Sample Source

Human genomic DNA from a lymphoblastoid B-cell line (NA10860) areobtained from the Coriell Institute for Medical Research. Genomic DNAfrom the pre-B acute lymphoblastoid leukemia cell line REH (22) isisolated using the AllPrep Universal kit (Qiagen). DNA is quantifiedusing the Qubit dsDNA BR Assay Kit (Thermo Fisher Scientific).

Protocol for Whole Genome Bisulphite Sequencing Library PreparationAccording to One Embodiment of the Present Invention

Adapter Annealing

Oligonucleotides are purchased from Integrated DNA Technologies. The3′-adapter, ss1 (5′-GACGTGTGCTCTTCCGATCT-3′ -amino-modifier (SEQ IDNO:1) (ss1-A) and 5′P-AGATCGGAAGAGCACACGTC (SEQ ID NO:2) (ss1-B)) and5′-adapter ss2 (5′-ACACGACGCTCTTCCGATCT (SEQ ID NO:3) (ss2-A) and5′-AGATCGGAAGAGCGTCGTGT) (SEQ ID NO:4) (ss2-B)) are prepared by mixingthe two oligonucleotides in the adapter pair to a final concentration of100 μm in 50 μL of 100 mM NaC1, 10 mM Tris-HCl (pH 8.0), 0.5 mM EDTA.The oligonucleotides are annealed by heating the mixture to 95° C. andslowly decreasing the temperature to 10° C.

Library Construction

Genomic DNA is sheared to 300-400 bp (Covaris E220 System) and treatedwith sodium bisulphite (EZ DNA Methylation Gold, Zymo Research). Theconverted DNA is first treated with 5 units of polynucleotide kinase(Thermo Fisher Scientific), in T4 DNA ligase buffer (see buffercomposition below) in a total volume 15 for 15 min at 37° C. Thereaction mixture is heated to 95° C. for 3-5 min in a thermal cyclerwith a heated lid and then cooled on an ice/water bath. For the 3′-endligation; adapter ss1 (final conc 10 μM), T4 DNA ligase buffer (40 mMTris-HCl pH 7.8.10 mM MgCl₂, 10 mM DTT, 0.5 mM ATP), PEG4000 (5% w/v)and 30 units T4 DNA ligase (Thermo Fisher Scientific) and nuclease freewater is added to the sample on ice, in a total volume of 30 μl.Ligation reaction mixtures are incubated at 20° C. for 1 h, andsubsequently purified using AMPure XP (BeckmanCoulter) beads in a 2:1bead to sample ratio and eluted with 10 μl nuclease free water. Theeluted DNA is heated to 95° C. for 3-5 min in a thermal cycler with aheated lid and then cooled on an ice/water bath. For the 5′-endligation; ss2 (final conc 10 μM), T4 DNA ligation buffer, PEG4000 (5%,w/v) and 30 units T4 DNA ligase (Thermo Fisher Scientific) and nucleasefree H₂O is added to the sample on ice, in a total volume of 20 μl.Ligation reaction mixtures are incubated at 20° C. for 1 h, purifiedusing AMPureXP beads in a 2:1 bead to sample ratio and eluted in 10 μlnuclease free water. The libraries are amplified for 4 cycles using KAPAHiFi Uracil+ ReadyMix (KAPA Biosystems) and oligonucleotides:

(SEQ ID NO: 5) 5'-AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACG CTCTTCCGATCT-3' (PCR Universal primer),  (SEQ ID NO:6)5'-CAAGCAGAAGACGGCATACGAGATNNNNNNGTGACTGGAGTTCAGA CGTGTGCTCTTCCGATCT-3' where NNNNNN denotes the Illumina index barcode sequence. The finallibraries are purified twice with AMPure XP beads using a 1:1 bead tosample ratio.Sequencing Libraries

The EZ DNA Methylation Gold kit is used for sodium bisulphite conversionof DNA according to the specifications specific for each library type asdescribed below.

Conventional WGBS libraries are prepared using the NEBNextUltra kit.Briefly, 1 μg of gDNA is sheared to 300-400 bp (Covaris E220 system).End repair, A-tailing and ligation of methylated adapters is performedaccording to the manufacturer's protocol with the following minormodifications: ligated samples are cleaned using AMPure XP beads at a2:1 bead to sample ratio prior to bisulphite conversion and PCRamplified for six cycles using the KAPA HiFi Uracil+ PCR polymerase.

The ‘post-bisulphite’ conversion WGBS libraries are prepared accordingto the Accel-NGS Methyl-Seq DNA library kit (Swift BioSciences) or theTruSeq DNA Methylation Kit (Illumina) according to the manufacturers'protocols. The Accel-NGS libraries are generated from 100 ng of sheared(350 bp, Covaris E220 System) gDNA that is subsequently bisulphiteconverted. Four cycles of PCR are used to amplify the Accel-NGSMethyl-Seq libraries. The TruSeq DNA Methylation libraries are generatedfrom 100 ng of sodium bisulfite treated gDNA without pre-shearing. Ninecycles of PCR are used to amplify the TruSeq DNA Methylation libraries.

RRBS libraries are prepared by a single-tube workflow using NEBNextUltrareagents (NEBNextUltra EndRep/A-tailing module, Ligation module andMethylated Adapters, New England Biolabs). Briefly, 200 ng of gDNA in atotal volume of 25 μl is digested for 16 h using 50 units of MspI inNEB2 buffer (New England Biolabs). After the incubation the reactionmixture is transferred to an end repair/A-tailing reaction mixture. Endrepair, A-tailing and ligation of methylated adapters are performed asrecommended in the NEBNextUltra kit protocol. The adapter concentrationsare reduced 10-fold in the ligation mixes (50 nM final concentration)compared to the manufacturer's instruction to avoid excessive formationof adapter dimers. After ligation the samples are purified with AMPureXP beads applying a 2:1 bead to sample ratio, prior to bisulphitetreatment. Bisulphite-converted libraries are PCR amplified for elevencycles using the Pfx Turbo Cx polymerase (Agilent Technologies). Twoconsecutive bead purifications with a 0.9:1 bead to sample ratio areperformed to clear the PCR-amplified libraries from oligonucleotides andadapter dimers.

SureSelect Methyl-Seq (Agilent Technologies) libraries are prepared from3 μg of gDNA following the manufacturer's protocol.

Sequencing and Data Analysis

Paired end sequencing (2×125 bp) is performed on a HiSeq2500 systemusing the TruSeq v4 chemistry (Illumina). The specific parameters forthe programs used for mapping, quality assessment, and DNA methylationcalling are provided in detail in FIG. 2.

As shown in WGBS process 200 of FIG. 2, sequence data is obtained atstep 210. At step 220, adapter trimming and quality filtering of readsis performed with TrimGalore v0.37 (minimum adapter overlap of 1 bp andQ score cut off 20) specifying options; —paired, —trim1 AccelNGSMethyl-Seq reads are additionally trimmed 18 base pairs at the beginningof each read2 and at the end of each read1 by specifying options;—clip_R2 18 and —three_(—)prime_clip_R1 18. At step 230, alignment tothe reference genome is performed with Bismark v0.14 (bowtie2) using thedefault parameter settings. At steps 240 and 250, PCR duplicates areremoved using the Bismark deduplication script and data from technicalreplicates is merged with Samtools. At step 260, GC bias and readcoverage is analysed using Picard Tools, BEDTools v2.23.0 and Qualimap.At step 270, methylation calling is performed with Bismark specifyingoptions; —no_overlap, —ignore and —ignore_r2. The decision if to excluderesidues in the beginning or end of reads is based on the Mbias profileof each library (see FIG. 21). At step 270, methylation values on plusand minus strands ware combined using Bismarks coverage2cytosine option,specifying; —merge_CpG or alternatively by a custom R script. At steps280 and 290, correlation of methylation and CpG site coverage isanalysed from the Bismark output files using custom R scripts.

Briefly, quality control of sequencing data is performed with the FastQCtool. Sequence reads are quality filtered and adapters are trimmed usingTrimGalore. Alignment to the human reference assembly GRCh37 andmethylation calling is performed with the Bismark v 0.14 software (23)and the pipeline tool ClusterFlow v 0.4 http://www.clusterflow.io. GCbias metrics in sequencing data is analysed with Picard Tools(http://broadinstitute.github.io/picard/). Sequencing coverage acrossthe whole genome and in genomic features is determined with Qualimap(24) and BEDTools (25). CpG site coverage and concordance of methylationcalls is computed from the Bismark methylation extractor output filesusing custom R scripts. The cytosine methylation status is called perindividual CpG sites as #C/(#C+#T) for CpG sites with at least 5×coverage. Thus methylation is detected if at least one methylated readis observed. CpG sites are annotated using BEDTools. Annotation filesare downloaded from the UCSC Genome Browser or prepared from the GENCODEhg19 annotation by methods similar to those described in;https://www.gitbook.com/book/ycl6/methylation-sequencing-analysis.Hypomethylated regions are identified using MethylSeekR (26) andoverlapping hypomethylated regions are determined using the‘findoverlaps’ function in the R package GenomicRanges using defaultsettings (27).

Example 2

Processing of Accel-NGS Methyl-Seq Reads

A low complexity tag of varying length is added to the 3′ termini of thessDNA during the Accel-NGS Methyl-Seq library preparation (see FIGS. 1,3 and 4), and these sequence tails are present at the beginning of allsecond read (R2) sequences. Since paired-end sequencing read lengths of125 base pairs are close to the insert sizes of the libraries, theadditional sequence tails in the Accel-NGS Methyl-Seq libraries arepresent at the end of many of sequences from the first read. The kitvendor suggests that trimming off 10 residues at the beginning of eachR2 sequence and end of each R1 sequence for read lengths over 100 bpshould be sufficient to remove most of the artificial sequence in thedata. However, based on per base sequence content plots (see FIGS. 3 and4 for per base sequence content plots for all WGBS methods) it isapparent that in this Accel-NGS Methyl-Seq data, the low complexitysequence tag may be up to 15-18 nucleotides in length. Thus trimming thefirst 18 residues of each R2 sequence and the end of each R1 sequence isperformed to avoid methylation artefacts and improve alignmentefficiency. FIGS. 3 and 4 show per base sequence content plots for theWGBS methods generated by the FastQC program. In FIG. 3, the X-arisshows the position in the read and the Y-axis shows the % of all bases.In FIGS. 3 and 4, green (indicated by arrow 352)=A, blue (indicated byarrow 354)=C, red (indicated by arrow 356)=T, black (indicated by arrow358)=G. In plots 310 and 320 of FIG. 3, plots 330 and 340 of FIG. 3 andplots 430 and 440 of FIG. 4, are shown for adapter trimmed reads. Inplots 410 and 420 of FIG. 4, is visualized that a low complexitysequence tag is added to the 3′end of single stranded bisulfiteconverted DNA during Accel-NGS Methyl-Seq library prep. Judged by theread 2 profile, a tail trimming of 15-18 residues is required to removeall artifacts from the library preparation.

DNA Methylation Analysis Using 450 k Bead Arrays

Genomic DNA (500 ng) is treated with sodium bisulphite (EZ DNAMethylation Gold) and the DNA methylation levels are measured using theInfinium HumanMethylation 450 k BeadChip Array (Illumina) according tothe manufacturer's instructions. Raw beta-values are extracted from thearrays using the Genome Studio Methylation Module (Illumina) andmethylation data from probes that hybridize to more than one genomiclocation and from probes with SNPs in the target regions of their3′-ends are filtered out as previously described (28).

Splinted Adapter Tagging (SPLAT) for Whole Genome Bisulphite SequencingLibrary Preparation

Embodiments of the present invention may also be used to provide SPLAT,which is an alternative method that introduces a new concept forefficient ligation of sequencing adapters to bisulphite converted singlestranded DNA fragments. The SPLAT method takes advantage of splintoligonucleotides (29) to create short stretches of dsDNA fragments thatallow subsequent ligation of sequencing adapters using standard dsDNAligation with T4 DNA ligase, which is more efficient than ligation ofssDNA. SPLAT, which is outlined in FIG. 1 (together with the otherlibrary methods for WGBS) is a sensitive method, which uses affordableoff-the-shelf enzymes. Using SPLAT with 100 ng of input DNA subjected toonly four PCR amplification cycles (using KAPA HiFi Uracil+ polymerase)yields sufficient amounts of library for WGBS. Library size profiles andthe results from library quantifications are shown in FIGS. 5, 6 and 7.The volume of the final libraries is 20 μl and the concentrations shownin the plots are determined using a Tape Station instrument. FIGS. 5 and6 show size profile plots of WGBS libraries generated with fourdifferent methods: Size profile 510 of FIG. 5 is for the lymphoblastoidB-cell line NA10860 generated by TruSeq DNA Methylation. In FIG. 5, theX-axis shows the size in base pairs and the Y-axiss shows sampleintensity in fluorescence units. Size profile plot 520 of FIG. 5 is forthe B-cell leukemic cell line REH generated by TruSeq DNA Methylation.Size profile plot 530 of FIG. 5 is for the lymphoblastoid B-cell lineNA10860 generated by a SPLAT method according to one embodiment of thepresent invention. Size profile plot 540 of FIG. 5 is for the B-cellleukemic cell line REH generated by a SPLAT method according to oneembodiment of the present invention. Size profile plot 610 of FIG. 6 isfor the lymphoblastoid B-cell line NA10860 generated by Accel-NGS. Sizeprofile plot 620 of FIG. 6 is for the B-cell leukemic cell line REHgenerated by Accel-NGS. Size profile plot 630 of FIG. 6 is for thelymphoblastoid B-cell line NA10860 generated by NEBNextUltra. Sizeprofile plot 640 of FIG. 6 is for the B-cell leukemic cell line REHgenerated by NEBNextUltra.

FIG. 7 shows size profile plots of eight SPLAT libraries generated fromthe lymphoblastoid cell lines NA11992 and NA11993. Profile plots 710 and730 are for the gDNA (1000 ng) sheared to 300-400 bp using a CovarisE220 system (profile plots are shown prior to bisulfite conversion).Profile plots 720 and 740 are for the SPLAT library (color codedaccording to which sheared DNA they are derived from) using 100 ng ofsheared and bisulfite converted gDNA. Libraries are PCR amplified for 4cycles (KAPA HiFi Uracil+). The final volume of each library is 20 uland the concentration (as measured by TapeStation) is 3-7 nM.

After bisulphite conversion, short double stranded adapters (20nucleotides) comprising a random 3′ overhang are annealed to the 3′ endsof the ssDNA and ligated using T4 DNA ligase. Similarly in a secondstep, the 5′ ends of the ssDNA are ligated using adapters comprising arandom 5′ overhang. To prevent self-ligation of adapters in the firstligation step, an amino modification (3′ Amino Modifier, Integrated DNATechnologies) is added to the 3′-terminal nucleotide in the randomhexamer oligo. In the second ligation step the oligo modification is notrequired. The libraries are subsequently amplified by PCR making use ofthe KAPA HiFi Uracil+ polymerase, which is capable of reading the uracilbase and is compatible with oligos that contain Illumina flow cellbinding and indexing sequences.

The SPLAT method according to one embodiment of the present invention isvalidated by performing WGBS of DNA from two different sources, namelythe lymphoblastoid B-cell line NA10860 and the B-cell leukemic cell lineREH (22). These two cell lines, an immortalized B-cell line and a cancercell line are chosen to mirror samples with differing methylationprofiles. Two SPLAT libraries are prepared from each cell line and eachlibrary is sequenced on one lane, PE125 base pairs using a HiSeq2500machine (in total four SPLAT libraries). Data yields and mappingefficiencies are in the expected range for WGBS and the PCR duplicationlevels are very low (1-2%) in all four SPLAT libraries. Sequencinginformation, mapping efficiencies and PCR duplication levels are listedin Table 1 of FIG. 8. Data from the two technical replicates per celltype are merged prior to analysis and the final average read coverage is16× and 22× in NA10860 and REH data, respectively. At CpG dinucleotidepositions specifically, the average coverage is 13× and 17× in NA10860and REH SPLAT data, respectively (Table 2 of FIG. 9). The SPLATlibraries from both cell types displayed uniform genome coverage, albeitcoverage decreases in CpG islands and in very GC rich promoter regions(see FIG. 10). This is a commonly observed phenomenon in next generationsequencing (NGS) data and is thought to be a consequence of low PCRefficiency for GC-rich regions. In summary, WGBS libraries prepared withthe SPLAT method display excellent global performance metrics such asdata yield, mapping efficiency, PCR duplication rates and uniformity ofcoverage.

Validation of Methylation Calls in SPLAT Data Against High CoverageReference Data Sets:

To obtain high coverage ‘reference’ methylation maps for both cell linesNA10860 and REH, WGBS data is merged from six sequencing libraries thatare prepared using three different commercial kits (TruSeq DNAMethylation, Accel-NGS Methyl-Seq, NEBNextUltra). In this way two highcoverage WGBS data sets are created with average read coverages of ˜50×for use as reference data sets for the results from SPLAT (see Table 2of FIG. 9). The concordance of methylation profiles between SPLAT andthe reference data sets are investigated by comparing methylation levelscomputed across reads at individual CpG sites. To measure how the readcoverage in SPLAT affects the accuracy of DNA methylation calls CpGsites are binned by coverage and measured the correlation with themethylation levels called in the high coverage reference data set forCpG sites with ≥20× coverage (see Table 3 of FIG. 11).

As might be expected, the methylation calls are more accurate withincreasing read-depth, however still at low coverage the correlationcoefficient is >0.9. When comparing all CpG sites interrogated by fiveor more reads Pearson's R is 0.94 for NA10860 and 0.97 for REH. Pairwisecomparisons are performed of methylation levels between SPLAT and thereference data sets from NA10860 and REH for CpGs located in CpGislands, putative enhancer regions and known repetitive elements (seeplots 1312, 1314, 1316, 1322, 1324 and 1326 of FIG. 13). The mean readcoverage of the CpG sites in these regions is shown in Tables 1330 and1340 of FIG. 13. To investigate regions with intermediate methylationlevels methylation levels are also compared at individual CpG siteslocated within 36 known imprinted regions where one of the alleles isexpected to be fully methylated while the other is fully unmethylated(30). In the lymphoblastoid cell line (NA10860) a large fraction of theCpG sites located in the known imprinted regions displayed the expectedmethylation levels close to 50%. However, in the cancer cell line (REH)aberrant DNA methylation profiles that are indicative of loss ofimprinting are observed (see FIG. 12). This is a common phenotype ofcancer cells (31). FIG. 12 shows a comparison of methylation levels atindividual CpG sites located throughout known imprinted regions in thehigh coverage reference data sets (y axis) and in SPLAT libraries(x-axis). FIG. 13 show a comparison of SPLAT with a high coveragereference dataset. Pairwise comparison of methylation levels atindividual CpG sites in CpG islands, enhancers, and repetitive regionsdetermined by SPLAT (x-axis) and the high-coverage reference WGBS data(y-axis) obtained by combining the data from TruSeq DNA Methylation,Accel-NGS and NEBNextUltra libraries. Pearson's correlation coefficientsare shown in the lower right corner of each scatter plot are shown inplots 1312, 1314, 1316, 1322, 1324 and 1326 of FIG. 13. The mean readcoverage of the CpG sites in CpG islands, enhancers and repeats forSPLAT and the high coverage reference data set are shown in Tables 1330and 1340 of FIG. 13. Comparison of the numbers and overlaps ofun-methylated regions (UMRs) between SPLAT and high coverage referenceWGBS data are shown in diagrams 1350 and 1360 of FIG. 13. Comparison ofthe numbers and overlaps of lowly methylated regions (LMRs) in SPLAT andhigh coverage reference WGBS data are shown in diagrams 1370 and 1380 ofFIG. 13.

Hypomethylated Regions in Whole Genome Bisulfite Sequencing LibrariesPrepared with SPLAT:

An important aspect for determining the quality of a WGBS experiment isthe ability for unbiased, genome-wide detection of regulatory regions.Therefore, as a second approach to validate the data from SPLAT, theMethylSeekR software is used for identification of regions belonging toone of two distinct classes: CpG-rich, completely unmethylated regionsthat correspond to proximal regulatory sites including promoters (UMRs)and CpG-poor, low-methylated regions that correspond to distalregulatory sites (LMRs) (26). The UMRs detected in the SPLAT librariesand the high coverage reference data set are highly overlapping (seediagrams 1350 and 1360 of FIG. 13). In total, 97% and 93% of the UMRsdetected in NA10860 and REH cells, respectively, overlapped with thehigh coverage reference data set. Unlike UMRs, which contain regionswith a high density of CpG sites that typically are completelyunmethylated (mean methylation level 6.5%), LMRs are short regions withfew CpG sites with more intermediate methylation levels (mean 18-22%)that are thought to be associated with TF binding. In total 74% and 76%of the LMRs identified overlapped between SPLAT and the high coveragereference data set in NA10860 and REH cells, respectively (see diagrams1370 and 1380 of FIG. 13). As expected, more LMRs are detected in thehigh coverage data than in SPLAT. Notably however, the fractions of LMRsthat are uniquely identified in either data set is higher than thatobserved for the UMRs. For instance, in NA10860 cells 3722 LMRs areunique to the SPLAT data and 8700 LMRs are unique to the high coveragereference data. Because the uncertainty in estimation of methylationlevels is dependent on coverage, especially so in the regions thatdisplay intermediate methylation levels, the sequencing coverage atthese regions is looked at specifically. The average coverage of theregions with overlapping LMRs is 13-17× in the SPLAT libraries and 36×in the high coverage reference datasets. Despite this, when looking atthe regions specifically called in the high coverage data set, but notin the SPLAT libraries these are covered at the same average sequencedepth as the overlapping regions. When inspecting the non-overlappingregions in more detail it is found that the mean methylation levels aregenerally higher in the uniquely identified regions than in theoverlapping LMRs (mean 18-22% methylation in overlapping LMRs and 26-29%methylation in unique LMRs). Thus methylation levels across unique LMRsdeviated upwards towards software's upper limit cut-off for the defininga LMR (50% methylation), which may at least in part explain why theseregions are called in one data set, but not in the other.

Comparison of SPLAT to commercial whole genome bisulphite sequencingmethods. Next, the performance of SPLAT is assessed in individualcomparisons with the three commercial methods for bisulphite sequencinglibrary preparation. In two of the methods the DNA is bisulphite treatedprior to adapter ligation using reagents from the TruSeq DNA Methylation(formerly EpiGnome) kit and the Accel-NGS Methyl-Seq kit, and aconventional method (NEBNextUltra), which is based on adapter ligationprior to bisulphite treatment (see FIG. 1). The TruSeq DNA Methylationprotocol makes use of the PBAT concept with oligos with degenerate 3′ends for adapter tagging, whilst the strategy for adapter tagging inAccel NGS Methyl-Seq is based on Adaptase™ technology (see FIG. 1). Thetwo types of ‘post bisulphite’ WGBS libraries are prepared using 100 ngof input DNA, whilst 1000 ng of input DNA is used for the conventionalNEBNextUltra libraries.

Sequencing Metrics:

WGBS libraries are sequenced in one lane per technical replicate using aHiseq2500 instrument and 125 bp paired-end reads with v4 sequencingchemistry. Sequence reads from all libraries are pre-processed prior toalignment using the same parameters, with the exception of the Accel-NGSMethyl-Seq data that required additional processing to remove the lowcomplexity sequence tags that are introduced during library preparation.To avoid biases in the comparison, the same parameters are used foralignment of all libraries with the Bismark software (23). Mapping ratesare between 70% and 83% for each of the WGBS methods, which isacceptable as the reduced complexity of the reads is expected to have anegative impact on the alignment efficiency (see Table 1 of FIG. 8). Thehighest mapping efficiency (83%) is achieved for the SPLAT and Accel-NGSMethyl-Seq libraries. The PCR duplication rate is low for SPLAT,Accel-NGS Methyl-Seq and NEBNextUltra (1-2% per lane), while TruSeq DNAMethylation libraries displayed higher PCR duplication rates (12-17% perlane) (see Table 1 of FIG. 8).

Data from two technical replicates are merged prior to downstreamanalysis. The amount of sequence data generated, the data yield afteralignment and removal of PCR duplicates, the average coverage, and themean library insert sizes in the WGBS methods are listed in Table 4 ofFIG. 14 which shows performance metrics for WGBS library preparationmethods.

WGBS libraries have relatively short insert sizes and consequentlysuffer from significant adapter contamination, particularly when readlengths are ≥100 bp. It is observed that the shortest mean insert sizesof ˜160 base pairs in the TruSeq DNA Methylation libraries and meaninsert sizes between 170 and 195 bp for the other protocols(Supplementary Table S2). Lower mapping efficiencies, high duplicationrates, and short insert sizes are factors that all contribute toconsiderable loss of data in WGBS. The data yield relative to the amountof raw sequencing data generated is lowest for the TruSeq DNAMethylation libraries, where only 55-58% of data is retained afterpre-processing, alignment and de-duplication. The Accel-NGS Methyl-seqand NEBNextUltra libraries retained 65-71% of data (mean 68%). The SPLATmethod retains 65-76% of the data, which on average is the method thatretains the most data after filtering (see Table 4 of FIG. 14).Therefore, the average genome coverage ranges from 14× to 22× in theWGBS data sets. Prior to performing subsequent analyses, each of theWGBS data sets is down-sampled to approximately the same number of readpairs (218-219 M for NA10860 libraries, 211-216 M for REH libraries) toenable cross-method comparisons with the same amount of starting data.

Read Coverage of WGBS Libraries:

Most currently used next generation sequencing library preparationmethods result in an under-representation of GC-rich regions, whichoriginates at least in part, from PCR amplification (32,33). In WGBSdata, the GC bias tends to be even more pronounced than in standardsequencing libraries and thus important GC rich regions (CpG islands)that are targets of DNA methylation, e.g. in cancer can be significantlyunderrepresented. It is determined that the normalized read coverage in100 bp windows of increasing GC content in the human reference genome,and found that the methods for sequencing library preparation generatedistinct biased GC profiles (see plots 1510 and 1520 of FIG. 15). In theNEBNextUltra libraries, coverage is skewed towards AT rich regions,while GC rich regions are poorly covered. In contrast, in TruSeq DNAMethylation libraries coverage is skewed towards GC rich regions.Accel-NGS Methyl-Seq and SPLAT libraries had more uniform GC biasprofiles, where regions with extreme base compositions, either AT or GCrich, are underrepresented.

Sequence Bias in Whole Genome Bisulphite Sequencing Libraries

GC Bias Observed for the Different Methods:

The plots of FIG. 15 show the normalised coverage in 100 bp windows ofincreasing GC content in the human reference genome. NEBNextUltralibraries (see plots 1538 and 1548 of FIG. 15) have higher readcoverages in AT rich regions, whilst the TruSeq DNA Methylationlibraries (see plots 1532 and 1542 of FIG. 15) have increased readcoverage of GC rich regions. The AccelNGS Methyl-Seq and SPLAT libraries(see, respectively, plots 1536 and 1546, and plots 1534 and 1544, ofFIG. 15) display a lower GC bias, however regions with extreme GCcontent are not well represented.

Cumulative Coverage of Different Genomic Regions:

(Coverage plots in FIG. 15) for the whole genome are shown in green, CpGislands in purple, FANTOM5 enhancer regions in blue and a set of 1000promoter regions that are difficult to sequence due to high GC contentin grey.)

Next, the read coverage distribution generated by the WGBS librarypreparation methods between genomic regions is analyzed. Cumulativecoverage plots for the whole genome, enhancer regions as defined by theFANTOM5 consortium (34), CpG islands and a set of 1000 promoters thathave been characterized as ‘difficult promoters’, which have very highCG content and are notoriously difficult to sequence (35), are shown inplot 1520 of FIG. 15 for both cell types (see FIG. 10 for coveragehistograms). Examples of genome browser views for the NA10860 cell typeare shown in FIG. 16 to further illustrate coverage and methylationprofiles. As is already inferred based on the GC bias profiles, thecoverage of different genomic features varies in a characteristic mannerbetween the WGBS methods. Out of the four methods, the Accel-NGSMethyl-Seq and SPLAT libraries displayed the most uniform coverage ofthe whole genome and of enhancer regions. However, for both thesemethods, the read coverage dropped in CpG islands and a substantial dropin coverage is observed in the ‘difficult promoters’. The TruSeq DNAMethylation libraries displayed uneven overall coverage of the genome.However, GC-rich promoter regions and CpG islands generally displayedhigher coverage than the genome on average and this is the only methodthat obtained adequate coverage of the ‘difficult promoters’. TheNEBNextUltra libraries on the other hand are characterized both byuneven whole genome coverage and a severe decrease in coverage in CpGislands and ‘difficult promoters’. Importantly, the GC bias and coverageprofiles are very reproducible between the two different cell types foreach of the WGBS methods described here, which indicates these resultsare robust against any biological differences in total DNA methylationlevels (see FIG. 15).

Genome Browser Views Displaying Coverage and Methylation Tracks for theFour Different WGBS Libraries Generated from the NA10860 Cell Type:

The blue tracks represent the read coverage, the red tracks representthe methylation levels across the regions and the green bars at thebottom of the panels represent CpG islands for genome browser view 1610(read coverage and methylation levels across a 3.5 Mb region ofchromosome), for genome browser view 1620 (zoom-in view of a CpG poor7.3 kb intergenic region on chromosome 12; and for genome browser view1630 (zoom-in view of a 6.4 kb region containing a methylated CpG islandon chromosome 19.

Coverage Biases in Public WGBS Data Sets.

It should be noted that the findings presented herein representobservations in the laboratory at a given point in time. To investigateif the observed biases in genomic and CpG site sequence coverage arereproducible between labs and not only characteristic to the sequencinglibrary preparations, human WGBS data sets according to one embodimentof the present invention are downloaded from the NCBI Sequence ReadArchive (SRA) from different library preparation protocols and analysedtheir coverage profiles. See FIG. 17, which shows coverage profilesprofiles 1710, 1720 and 1730 of public WGBS data sets downloaded fromthe short read archive (SRA) for TruSeq DNA Methylation libraries fromlymphoblastoid cell line NA18507 (profile 1710 for Accession#SRR1867799, profile 1720 for SRR1867802, and profile 1730 SRR1818296);coverage profiles 1740, 1750 and 1760 of Conventional WGBS librariesamplified with the KAPA HiFi Uracil polymerase for SRR1045663:Spleen(profile 1740), SRR1045744:Bladder (profile 1750), and SRR1536575:HCT116colorectal cancer cell line (profile 1760); and coverage profiles 1770,and 1780 and 1790 of Conventional WGBS libraries amplified with thePfuTurbo Cx polymerase for SRR948844:B-lymphocytes (profile 1770),SRR096827: human stem cells 1 (profile 1780), and Tagmentation-WGBSlibrary SRR447397: lymphoblastoid cell line GM20846 (profile 1790).(Coverage plots in FIG. 17 for the whole genome are shown in green,enhancer regions in blue, CpG islands in purple, and a set of 1000promoter regions that are difficult to sequence due to high GC contentin grey).

First, three TruSeq DNA Methylation libraries from the humanlymphoblastoid cell line NA18507 obtained from the Blueprint consortium(GSE66285) are assessed in which it is observed the same trend towardsincreased coverage of CpG rich regions, including difficult promoters,as in our data. Second, five conventional human WGBS data setsoriginating from five various tissue types in which libraries areamplified using the two most commonly used uracil reading PCRpolymerases (KAPA HiFi Uracil+ or PfuTurbo Cx) and onetagmentation-based WGBS data set (18,36-38) are evaluated. The coverageprofiles from these libraries are very similar to those in librariesaccording to one embodiment of the present invention (see FIG. 15). Asin SPLAT, Accel-NGS Methyl-Seq and NEBNextUltra libraries, a commonfeature is a decline in coverage over CpG rich regions and difficultpromoters.

Determination of DNA Methylation Levels and Quality Control ofMethylation Calls:

Global methylation levels in the CHG and CHH (where H represents eitherA, T or C but not G) sequence context are low (0.3-1%), indicating thatthe bisulphite conversion rates are >99% in all libraries (see Table 5of FIG. 18, shows global cytosine methylation in CpG, CHH and CHGcontext).

An alternative method to assess bisulphite conversion rates is todetermine the methylation levels in mitochondrial DNA, which is presumedto be unmethylated in human samples (39). It is found that the averagemethylation levels across mitochondrial CpG sites are very low in theSPLAT, Accel-NGS Methyl-Seq and NEBNextUltra libraries as expected.However, the average mitochondrial CpG methylation levels originatingfrom TruSeq DNA Methylation libraries are consistently high (see Table 6of FIG. 19, which shows average methylation across mitochondrial CpGsites).

The reason for this bias is unknown, but could be due to incompletebisulphite conversion of the circular mitochondrial DNA. Furthermore,individual reads with two or more CpG sites are analyzed to determinethe concordance of the methylation state of each cytosine position in aCpG context in each read (see Table 7 of FIG. 20 which shows a summaryof each read methylation).

The proportion of reads with concordant methylation states is extremelysimilar between methods, however the proportion of reads available forsuch an analysis (containing ≥2 CpG sites) varied greatly between themethods, namely only 17-18% of the reads from NebNextUltra libraries,22-26% of Accel-NGS and SPLAT libraries, and 35-36% of TruSeq DNAMethylation libraries. This result mirrors the coverage bias discussedabove.

M-bias plots are frequently used for quality control of bisulphitesequencing data and are useful for detection of methylation biases atthe ends of sequence reads (40). In an unbiased sequencing library themethylation levels should be independent of read position, and thus themean methylation levels plotted against read position should form ahorizontal line. Only the SPLAT libraries are unbiased in thisparameter. FIG. 21 shows Mbias profiles. The decision whether to excludebases in the beginning of reads from the methylation calling is based onMbias profiles. Mean methylation is plotted against read position andnonbiased libraries should exhibit a horizontal line. In the TruSeq DNAMethylation libraries the first six residues of each read are excludedfrom the methylation calling. In NEBNextUltra libraries the first tworesidues of read2 are excluded. In Accel-NGS Methyl-Seq libraries thefirst 2 residues of read1 and the last residue of read2 are excluded (inaddition to trimming the cytosine tails). In SPLAT libraries no residuesare excluded from the methylation calling.

The M-bias profiles in the TruSeq DNA Methylation libraries fluctuate,particularly at the beginning of the reads. Thus to avoid biases inmethylation levels in the TruSeq DNA methylation libraries the first sixresidues of each read from methylation calling are excluded. TheNEBNextUltra libraries exhibits a sharp decrease in methylation levelsat the beginning of the second read, which is characteristic forconventional library preparation protocols where end repair of sheareddsDNA fragments is performed with unmethylated cytosines. Thus, thefirst two bases of each read from methylation calling are excluded. TheM-bias profiles for Accel-NGS Methyl-Seq libraries (after removing thesequence tails) also display a small dip in the beginning of the firstread and a spike at the end of the second read and accordingly thesethree bases are excluded from the methylation calling.

Concordance of Methylation Levels Across Methods:

Next pair-wise comparisons are performed of the methylation levelscomputed across reads at individual CpG sites between methods for bothcell types (see Table 2610 of FIG. 25). First, the correlation betweenthe methylation levels are obtained by the WGBS methods and those with450 k Bead Arrays are measured. Using a minimum of 5-fold or highercoverage in the WGBS libraries, the concordance of methylation levelsbetween 450 k Bead Arrays and all WGBS methods is excellent (Pearson'sR=0.91-0.95 for NA10860 and 0.93-0.96 for REH). Concordance of themethylation levels across the four WGBS library preparation methods isalso high (Pearson's R=0.88-0.91 for NA10860 and 0.90-0.95 for REH),with the exception of the methylation levels originating fromNEBNextUltra libraries, which consistently displayed lower correlationcoefficients in all pair-wise comparisons. The correlation coefficientsfor comparison between technical replicates for each WGBS method aregiven in Table 8 of FIG. 22, which shows a correlation of methylationbetween technical replicates.

In the same pair-wise manner, there is also found a high degree ofcorrelation between the methylation levels determined by WGBS, RRBS, andthe SureSelect Methyl-Seq methods (Pearson's R=0.93-0.97 for NA10860 and0.95-0.98 for REH) (see Table 9 of FIG. 23, which shows sequence metricsfor RRBS and SureSelect MethylSeq libraries).

Generally, the correlation coefficients are higher for pair-wisecomparisons in the REH sample, presumably due to the fact that a largerproportion of the of the CpG sites in REH cells, compared to the normalB-cell line, are either completely methylated or unmethylated.Differences in methylation levels at individual CpG sites may be due todifferences in read coverage at the particular site, and therefore theconcordance of methylation levels across functionally different genomicregions was also assessed, which is less sensitive to variance in readcoverage. The concordance between regional mean methylation levelsacross CpG islands and FANTOM5 enhancer regions is high between WGBSmethods (Pearson's R=0.92-0.99),

FIG. 24 shows average methylation in CpG islands in scatterplots showingthe correlation of average methylation in CpG Islands, across WGBSlibrary preparation methods. Regions with an average CpG site coveragebelow 4× are excluded from the comparison.

FIG. 25 shows average methylation in enhancer regions in scatterplotsshowing the correlation of average methylation in FANTOM5 enhancerregions, across WGBS library preparation methods. Regions with anaverage CpG site coverage below 4× are excluded from the comparison.

The mean methylation levels across CpG islands showed excellentcorrelations (>0.99) in all comparisons between the ‘post bisulphite’WGBS methods. Similarly, for these methods the methylation levelcorrelation is also high across enhancer regions (Pearson'sR=0.94-0.97). Again, lower concordance is observed in the comparisonswith NEBNextUltra libraries (for enhancer regions; Pearson's R=0.92-0.96compared to 0.94-0.97 for comparisons solely between ‘post bisulfite’methods).

Concordance of Methylation Levels Across Methods:

Tables 2610 and 2612 of FIG. 26 shows pairwise comparison of methylationlevels at individual CpG sites, Pearson's correlation coefficients areshown to the left of the diagonal. The numbers of CpG sites (inmillions) included in each comparison are shown to the right of thediagonal. Venn diagrams 2630 and 2640 of FIG. 26 show the numbers andoverlaps of un-methylated regions (UMRs) detected in the three‘post-bisulphite’ library preparation methods. Venn diagrams 2650 and2660 of FIG. 26 show the numbers and overlaps of low methylated regions(LMRs) detected in the three ‘post-bisulphite’ library preparationmethods.

In summary, the ‘post bisulphite’ libraries yielded overall higherconcordance in methylation calls both between the WGBS libraries andeach of the other non-WGBS methods than the traditional WGBS method thatis used herein.

Comparison of Hypomethylated Regions in WGBS Libraries.

Next LMRs and UMRs are analyzed in the different WGBS data sets. In linewith the results described above, as many as 25% fewer UMRs and 50%fewer LMRs are detected in NEBNextUltra libraries compared to the othermethods (see Table 10 of FIG. 27, which shows numbers of low- andun-methylated regions as identified by MethylSeekR).

Therefore the overlap of LMRs and UMRs are only assessed in the ‘postbisulphite’ WGBS libraries. Between 90% and 96% of the UMRs detected inany given library overlapped with those detected in all of the libraries(Venn diagrams 2630 and 2640), therefore each of the ‘post bisulphite’methods are accurate in detecting UMRs (methylation level mean 6%,median 4%). Comparable numbers of LMRs are identified by all of the‘post bisulphite’ methods (27 475-28 438 for NA10860 and 51 828-59 023for REH, see Venn diagram 2660 of FIG. 26). Similar to what is describedin the previous section when comparing SPLAT to the high coveragereference data, the degree of overlap is lower (63-72%) than observedfor the UMRs. The greatest number of LMRs overlapped between the SPLATand Accel-NGS methods, presumptively due to the more evengenome-coverage achieved with these methods. However, when inspectingthe non-overlapping regions in more detail, despite that the coverage issimilar in the regions containing unique and overlapping LMRs (12-16×)across the WGBS methods, it is found that methylation levels of uniqueLMRs (mean methylation 26-29%) is on average 10% higher than in theoverlapping LMRs (mean methylation 16-20%).

Genome-Wide CpG Site Coverage Across Methods:

For each sequencing-based method and cell type the total number of CpGsites that are covered by five reads or more are measured (see Table 11of FIG. 28). The SPLAT and Accel-NGS Methyl-Seq data sets gave the bestoverall and most even coverage of the CpG sites in the human genome with88-90% of the total CpG sites covered by at least five reads. Thecorresponding proportions are 82-83% for TruSeq DNA Methylation and62-67% and NEBNextUltra. The results from the WGBS methods are alsocompared to RRBS and SureSelect Methyl-seq libraries where 8-10% and 14%of the total CpG sites are covered by at least five reads, respectively(see Table 11 of FIG. 28 and Table 9 of FIG. 23).

Moreover, CpG sites are identified that are under-represented in eachWGBS library by applying a coverage threshold of ≤2× and annotating theregions with poor coverage (see FIG. 30). Approximately 0.5 million CpGsites that are below this threshold are shared between all the ‘postbisulphite’ conversion libraries and are mainly annotated to intergenicregions, introns and repeats. Overall, the 3 M CpG sites with lowcoverage in TruSeq DNA Methylation libraries are over-represented inintrons, intergenic regions and repetitive elements. The SPLAT andAccel-NGS Methyl-Seq libraries had 1.3-1.5 and 1.5-1.6 M low coverageCpGs, respectively. As expected, in these libraries there are more lowcoverage sites in CpG islands and promoter regions (TSS±200 bp) comparedto TruSeq DNA Methylation libraries. The NEBNextUltra libraries had thelargest number of low covered CpG sites (4.7-6.0M) and a largeproportion of them are annotated to CpG islands and promoter regions,however many sites in intergenic regions and introns are alsoinsufficiently covered (see Table 12 of FIG. 29 which shows theannotation of low coverage CpGs (covered by two or fewer reads) togenomic features in NEBNextUltra libraries (216-219 M read pairsanalyzed)).

A coverage threshold of ≤2 reads is applied to identify CpG sites thatare insufficiently represented by the different WGBS library methods(based on down-sampled data). In TruSeq DNA Methylation libraries, lowcoverage sites are mostly found in intergenic regions and introns. TheSPLAT and Accel-NGS Methyl-Seq data displayed overall lower number ofCpG sites with low coverage, although the number of poorly representedsites in CpG islands and promoter regions are higher compared to theTruSeq DNA methylation libraries.

The greatest total number of CpG sites covered is obtained by the SPLATdataset followed by the Accel-NGS dataset (see Table 11 of FIG. 28).Moreover, these two protocols provided a better overall genome-widecoverage of CpG sites in repetitive elements, intergenic regions andintrons, which are the regions that provide the most important advantageof the WGBS approach over the other targeted methods.

WGBS of human samples are still costly to perform and thus the choice ofsample preparation method that will generate the largest amount usabledata is important. One must consider: (i) DNA input amount requirements;(ii) whether certain genomic regions/features are of particularinterest; (iii) cost efficiency; and (iv) whether the WGBS data willalso be used to assess genetic variation and/or copy number alterations,among others. An overall summary of the method evaluation can be foundin Table 13 of FIG. 31. The ‘post-bisulphite’WGBS library preparationmethods bring about a significant reduction in the required DNA inputand performed better than the traditional method in all of the metricspresented herein, thus providing a more economical alternative for WGBSespecially for scarce samples. In this study, the DNA input amount isset to 100 ng in order to obtain high quality methylation profiles forcomparison. However, for the SPLAT and Accel-NGS Methyl-Seq methods theamount of DNA input can be substantially decreased considering that for100 ng of input DNA, as few as four amplification cycles gave sufficientyield and that the PCR duplication rates are very low. The TruSeq DNAMethylation protocol on the other hand required more than twice as manyamplification cycles for the same input amount to obtain the same yield,and thus rather high PCR duplication rates limit the flexibility withrespect to input quantity.

One important aspect in choosing a WGBS method is bias in the regions ofthe genome covered. The SPLAT and Accel-NGS Methyl-Seq methods would bethe best if data from the largest number of CpG sites with most evencoverage over the genome is desired, especially if genetic variation(for example SNPs) will also be assessed from the WGBS data. In bothSPLAT and Accel-NGS Methyl-Seq data, some degree of coverage decline wasfound in CpG islands and in very GC rich promoter regions, which is acommon characteristic of many types WGBS data (Supplementary Figure S8).

Notably, the library preparation cost for SPLAT (<10 $/sample) is lessthan one tenth of the cost for any of the commercial WGBS methods,making SPLAT a particularly attractive method also for bisulphitesequencing of smaller genomes such as Arabidopsis and for applicationssuch as ChIP-bisulphite sequencing (ChIP-BS-seq) (43,44) where the costof library preparation per sample approaches the cost of sequencing. Thepost bisulphite adapter tagging (PBAT) method, which is the only otheralternative protocol for post bisulphite WGBS library preparation thathas been described in a peer-reviewed journal, has the advantage ofproducing amplification free libraries from low amounts of DNA. However,chimeric reads formed by joining of two distinct genomic regions in PBATlibraries often result in a low mapping efficiency (see online article;https://sequencing.qcfail.com/articles/pbat-libraries-may-generate-chimaeric-read-pairs).In contrast, our results suggest that chimeric reads is an issue thatoccurs using the original PBAT protocol and not in the methods describedhere. The mapping procedure used herein does not consider chimeric readpairs as valid alignments. Hence, the high mapping efficiencies forSPLAT as well as the other two post bisulphite methods (>70%)demonstrate that the contribution of chimeric fragments to the mappingefficiency estimation in these libraries is minor.

The TruSeq DNA Methylation method exhibited the best overall coverage ofCpG dense regions, such as promoters and CpG islands, however thismethod suffered from lower coverage of total CpG sites and more datadiscarded than the other methods. Thus if CpG dense regions are ofparticular interest, this would be the WGBS method of choice. Lastly,the conventional NEBNextUltra libraries required more input DNA,displayed poor coverage of CpG islands and promoter regions, andgenerally interrogated fewer CpG sites compared to the other methods andthus this method did not outperform any of the ‘post-bisulphite’methods.

The exact cause and origin of the method specific biases are stillunclear and multiple mechanisms may be involved. Differences in theefficiency of PCR amplification due to the sequence context andcomposition of the PCR buffer are recognized sources of coverage bias:DNA polymerases can differ in their ability to efficiently amplifyregions of extreme base composition. Hence the AT skewed coverage of theNEBNextUltra libraries in this study might be attributed to the use ofthe KAPA HiFi Uracil+ polymerase. On the contrary, the same polymeraseis used to amplify SPLAT libraries that did not display a similar typeof AT bias. Apart from PCR amplification, other causes of coverage biasmight be related to specific steps in the different protocols. Forinstance, non-random bisulphite-induced fragmentation in CpG denseregions might account for increased coverage of GC rich regions in theTruSeq DNA methylation libraries, by increasing the fraction of suchregions available for efficient adapter tagging. By contrast, biasedfragmentation of GC rich regions in the pre-sheared DNA used for SPLATand Accel-NGS protocols might lead to very short fragments that are lostin the library preparation. Moreover, secondary structure of singlestranded GC rich regions might negatively affect ligation or 3′-endtagging and contribute to the lower representation of such regions inSPLAT and Accel-NGS Methyl-Seq protocols.

The performance of WGBS methods may vary between labs and until across-laboratory comparison can be performed any recommendations basedon data produced by one lab only should be treated with caution. owever,the characteristics of the different library preparation methods arehighly reproducible across the two different cell types analysed. It ischosen to benchmark the methods using the large human genome, anapproach that is highly relevant for many researchers, althoughextensive benchmarking of a large number of samples and methods may beprohibited by the sequencing costs. However, by complementing ourbenchmarking with publicly available human WGBS data sets from severalexternal laboratories, the same type of coverage biases are observed inthe generated data and in the public data (see FIG. 17).

In summary, all ‘post bisulphite’ library preparation methods performbetter than the conventional library preparation method. Concordance ofmethylation levels across the different methods are high, both at thelevel of individual CpG sites and across regions. Since no method iscompletely free from sequence bias, the method of choice depends on theaim of the study and the scientific questions asked. As will be evidentto persons having ordinary skill in the art, the inventive methoddescribed hereinoffers a straightforward and highly cost efficientapproach for WGBS with results which compare favourably to existingmethods.

Experimental Protocol. Oligos: (Standard Desalted)

Materials:

Adapter ss1 oligos

(SEQ ID NO: 1) 5′-GACGTGTGCTCTTCCGATCTNNNNNN-3′ Amino Modifier(IDT) (ss1-A) (SEQ ID NO: 2) 5′Phos-AGATCGGAAGAGCACACGTC (ss1-B)

Adapter ss2 oligos

(SEQ ID NO: 3) 5′-ACACGACGCTCTTCCGATCT (ss2-A) (SEQ ID NO: 4)5′-NNNNNNAGATCGGAAGAGCGTCGTGT (ss2-B)

PCR oligos: universal and index oligos (25 μM stock)

(SEQ ID NO: 5) 5′-AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT-3′ (PCR Universal primer), (SEQ ID NO: 6)5′-CAAGCAGAAGACGGCATACGAGATXXXXXXGTGACTGGAGTTCAGACGTGTGCTCTTCCGATCT-3′ (PCR Index primer),

Adapter Annealing:

-   -   100 pmol/μl final (of each oligo)=100 μM    -   1 μl NaCl (5M)    -   1 μl 20×TE buffer    -   H₂O up to 50 ul    -   Heat to 95° C. and stepwise decrease temperature to 4-10° C.    -   Shearing and bisulfite conversion:    -   Shear DNA to 300-400 bp (Covaris).    -   Bisulfite conversion with the Zymo EZ DNA Methylation-Gold Kit        and elute in 10 μl.    -   PNK treatment (15 μl total volume)    -   10 μl DNA    -   1 μl T4 ligase buffer (30 U/μl Thermo Fisher Scientific)    -   3.5 μl nuclease free H₂O    -   0.5 μl PNK (10 U/μl Thermo Fisher Scientific)    -   37° C. for 15 minutes, 95° C. for 3-5 minutes and then place        directly on ice/water bath until cool (˜5 min) and proceed        directly to the next step.    -   Ligation 1 (30 μl total volume)    -   Add (in the following order):    -   15 μl DNA mix    -   3 μl adapter ss1    -   5 μl nuclease free H₂O    -   3 μl 10×T4 ligase buffer (Thermo Fisher Scientific)    -   3 μl PEG4000 (10× solution Thermo Fisher Scientific)    -   1 μl T4 ligase (30 U/μl Thermo Fisher Scientific)    -   Spin down briefly and incubate in thermocycler, 20° C. for 1 hr    -   Clean up with 60 μl AMPure beads and elute in 10 μl nuclease        free H2O. SAFE STOP (−20° C.)    -   Ligation 2 (20 μl total volume)    -   Denature for 3-5 min at 95° C. and then place directly on        ice/water bath until cool (˜5 min)    -   Add (in the following order):    -   10 μl purified DNA from previous step    -   2 μl adapter ss2    -   3 μl H₂O    -   2 μl 10×T4 ligase buffer (Thermo Fisher Scientific)    -   2 μl PEG4000 (10× solution Thermo Fisher Scientific)    -   1 μl T4 DNA ligase (30 U/μl Thermo Fisher Scientific)    -   Spin down briefly and incubate in thermocycler, 20° C. for 1 hr    -   Clean up with 50 μl AMPure beads and elute in 10 μl H2O. SAFE        STOP (−20° C.)    -   PCR    -   1 ligated DNA    -   25 μl 2×KAPA HiFi Uracil+ MasterMix    -   1 μl universal oligo (25 μM stock conc)    -   1 μl index oligo (25 μM stock conc)    -   13 μl H₂O    -   95° C., 3 min    -   98° C., 15 s    -   60° C., 30 s    -   72° C., 2 min    -   4-5 cycles    -   72° C., 5 min

Clean up with 1:1 AMPure beads and elute in 20 μl H₂O or 10 mM Trisbuffer. A small peak at ˜60 bp corresponding to residual oligos may beobserved if only one bead purification is performed after PCR.

Although no disturbance in sequencing has been observed due to this,however a second bead purification may be performed to remove themajority of the residual oligos if desired. If a second beadpurification is performed, elute the DNA from the 1st purification in 50μl (water or 10 mM Tris buffer) and do a final cleanup with 1:1 AMPurebeads. Elute in 20 μl H2O or 10 mM Tris buffer.

Reagents/Supplies Required:

-   -   Covaris microtubes    -   Zymo EZ DNA Methylation Gold kit    -   T4 DNA ligase HC 30 U/ul (Thermo Fisher Scientific)    -   PEG4000 (10× solution included with T4 DNA ligase from Thermo        Fisher Scientific)    -   PNK (10 U/μ ThermoFisher Scientific)    -   KAPA HiFi Uracil+ PCR 2× Master Mix (KAPA Biosystems)    -   AMPure XP beads (BeckmanCoulter)    -   80% ethanol    -   Nuclease free water

This protocol is validated by NGS using 100 ng DNA as the input amountand the KAPA HiFi Uracil+ enzyme (4-5 PCR cycles). The method could beperformed using other PCR polymerases. Yields from 4-8 nM (with 100 nginput DNA, 4 PCR cycles, final volume 20 μl) are routinely observed,when using high quality gDNA from cell lines. With gDNA samples fromprimary cells/tissue, which may be of lower quality, yields could belower.

While the foregoing invention has been described in some detail forpurposes of clarity and understanding, it will be clear to one skilledin the art from a reading of this disclosure that various changes inform and detail can be made without departing from the true scope of theinvention. For example, all the techniques and apparatus described abovemay be used in various combinations. All publications, patents, patentapplications, or other documents cited in this application areincorporated by reference in their entirety for all purposes to the sameextent as if each individual publication, patent, patent application, orother document are individually indicated to be incorporated byreference for all purposes.

All documents, patents, journal articles and other materials cited inthe present application are hereby incorporated by reference.

Although the present invention has been fully described in conjunctionwith several embodiments thereof with reference to the accompanyingdrawings, it is to be understood that various changes and modificationsmay be apparent to those skilled in the art. Such changes andmodifications are to be understood as included within the scope of thepresent invention as defined by the appended claims, unless they departtherefrom.

In addition, the purpose of the Abstract of the Disclosure in thisapplication is to enable the U.S. Patent and Trademark Office, as wellas the public generally, including any scientists, engineers andpractitioners in the art who may not be familiar with patent or otherlegal terms or phraseology to determine the what the technicaldisclosure of the application describes. Accordingly, while the Abstractof the Disclosure may be used to provide enablement for the followingclaims, it is not intended to be limiting as to the scope of thoseclaims in any way.

Finally, it is the applicants' intent that only claims which include theexpress language “means for” or “step for” be interpreted under 35U.S.C. § 112, paragraph 6. Accordingly, claims that do not expresslyinclude the phrase “means for” or “step for” are not to be interpretedas being within the purview of 35 U.S.C. § 112, paragraph 6, or to beconstrued as being subject to any case law interpreting the meaning ofthese phrases.

REFERENCES

The following references are referred to above by number in parenthesesand are incorporated herein by reference:

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What is claimed is:
 1. A method comprising the following steps: (a)forming a single stranded treated DNA by treating a double stranded DNAwith bisulfite, wherein the bisulfite denatures the double strand DNAand converts non-methylated cytosines in the double stranded DNA intouracils and leaves methylated cytosines in the double stranded DNAunchanged; (b) ligating a first adapter to a 3′ end of the singlestranded treated DNA, thereby forming a once adapter ligated nucleicacid strand, the first adapter comprising a double stranded nucleic acidcomprising a top strand and a bottom strand and having a firstsingle-stranded protruding random sequence that is at least 3 bases longand is located at the 3′ end of the bottom strand, the firstsingle-stranded protruding random sequence of the first adapter beingmodified at a 3′ end of the bottom strand to prevent self-ligation ofthe first adapter, and acting as a splint to join the single strandedtreated DNA with the first adapter, wherein, in the once adapter ligatednucleic acid strand, a 5′ end of the top strand of the first adapter isligated to the 3′ end of the single stranded treated DNA and the firstsingle-stranded protruding random sequence hybridizes with the singlestranded treated DNA; (c) ligating a second adapter to a 5′ end of theonce adapter ligated nucleic acid strand, thereby forming a twiceligated nucleic acid strand, the second adapter comprising a doublestranded nucleic acid comprising a top strand and a bottom strand andhaving a second single-stranded protruding random sequence that is atleast 3 bases long and is located at the 5′ end of the bottom strand,the second single-stranded protruding random sequence acting as a splintto join the once adapter ligated nucleic acid strand with the secondadapter, wherein, in the twice ligated nucleic acid strand, a 3′ end ofthe top strand of the second adapter is ligated to the 5′ end of theonce adapter ligated nucleic acid strand and the second single-strandedprotruding random sequence hybridizes with the once adapter ligatednucleic acid strand; and (d) performing a polymerase chain reaction(PCR) on the twice ligated nucleic acid strand, thereby generatingcopies of the twice ligated nucleic acid strand.
 2. The method of claim1, wherein the double-stranded DNA is a sheared double-stranded DNA froma longer double-stranded DNA.
 3. The method of claim 2, furthercomprising the step of shearing the longer double-stranded DNA.
 4. Themethod of claim 1, wherein the first protruding random sequence of step(b) and the second protruding random sequence of step (c) are 3 to 20bases long.
 5. A method comprising the following steps: (a) providing aRNA; (b) ligating a first adapter to a 3′ end of the RNA, therebyforming a once adapter ligated nucleic acid strand, the first adaptercomprising a double stranded nucleic acid comprising a top strand and abottom strand and having a first single-stranded protruding randomsequence that is at least 3 bases long and is located at the 3′ end ofthe bottom strand, the first single-stranded protruding random sequenceof the first adapter being modified at a 3′ end of the bottom strand toprevent self-ligation of the first adapter, and acting as a splint tojoin the RNA with the first adapter, wherein, in the once adapterligated nucleic acid strand, a 5′ end of the top strand of the firstadapter is ligated to the 3′ end of the RNA and the firstsingle-stranded protruding random sequence hybridizes with the RNA; (c)ligating a second adapter to a 5′ end of the once adapter ligatednucleic acid strand, thereby forming a twice ligated nucleic acidstrand, the second adapter comprising a double stranded nucleic acidcomprising a top strand and a bottom strand and having a secondsingle-stranded protruding random sequence that is at least 3 bases longand is located at the 5′ end of the bottom strand, the secondsingle-stranded protruding random sequence acting as a splint to jointhe once adapter ligated nucleic acid strand with the second adapter,wherein, in the twice ligated nucleic acid strand, a 3′ end of the topstrand of the second adapter is ligated to the 5′ end of the onceadapter ligated nucleic acid strand and the second single-strandedprotruding random sequence hybridizes with the once adapter ligatednucleic acid strand; and (d) performing an amplification reaction on thetwice ligated nucleic acid strand, thereby generating copies of thetwice ligated nucleic acid strand.
 6. A method comprising the followingsteps: (a) forming a single stranded treated DNA by treating a singlestranded DNA with bisulfite, wherein the bisulfite convertsnon-methylated cytosines in the single stranded DNA into uracils andleaves methylated cytosines in the single stranded DNA unchanged; (b)ligating a first adapter to a 3′ end of the single stranded treated DNA,thereby forming a once adapter ligated nucleic acid strand, the firstadapter comprising a double stranded nucleic acid comprising a topstrand and a bottom strand and having a first single-stranded protrudingrandom sequence that is at least 3 bases long and is located at the 3′end of the bottom strand, the first single-stranded protruding randomsequence of the first adapter being modified at a 3′ end of the bottomstrand to prevent self-ligation of the first adapter, and acting as asplint to join the single stranded treated DNA with the first adapter,wherein, in the once adapter ligated nucleic acid strand, a 5′ end ofthe top strand of the first adapter is ligated to the 3′ end of thesingle stranded treated DNA and the first single-stranded protrudingrandom sequence hybridizes with the single stranded treated DNA; (c)ligating a second adapter to a 5′ end of the once adapter ligatednucleic acid strand, thereby forming a twice ligated nucleic acidstrand, the second adapter comprising a double stranded nucleic acidcomprising a top strand and a bottom strand and having a secondsingle-stranded protruding random sequence that is at least 3 bases longand is located at the 5′ end of the bottom strand, the secondsingle-stranded protruding random sequence acting as a splint to jointhe once adapter ligated nucleic acid strand with the second adapter,wherein, in the twice ligated nucleic acid strand, a 3′ end of the topstrand of the second adapter is ligated to the 5′ end of the onceadapter ligated nucleic acid strand and the second single-strandedprotruding random sequence hybridizes with the once adapter ligatednucleic acid strand; and (d) performing a PCR on the twice ligatednucleic acid strand, thereby generating copies of the twice ligatednucleic acid strand.